Associated Genes:

Predicted to be deleted or partially deleted - AnxB9, Atpalpha, Calx, KaiR1D, Grik, hdly, CG5697, Tbc1d22, Brat1, HHEX, CG7079, Alp5, Ktl, CG12278, CG15695, CG15696, CG17270, CG17271, CG17272, Adss, peg, Jhbp15, Syp, CG31189, CG31191, CG31195, CG31207, CG31223, CG43446, Cortactin, Dhc93AB, dmrt93B, Fancd2, Ir93a, mir-1011, Mvl, r-l, Rab11, RhoGAP93B, Rlip, RpS20, RpS30, rtet, Sec15, snoRNA:CG31191-a, snoRNA:Psi18S-1295, snoRNA:Psi28S-2562, Synd, Takl1, TotA, TotB, TotC, TotX, TotZ, tRNA:Thr-CGT-1-3, tRNA:Thr-CGT-1-2, tRNA:Thr-CGT-1-1, asRNA:CR44106, asRNA:CR44047, lncRNA:CR44947, lncRNA:CR44048, lncRNA:CR44178, asRNA:CR46045

Comment: The deficiency chromosome retains the miniwhite marker from P{lacW}Rab11[j2D1] used in screen.
Map:

92F13;93B13, 3R:20762299;3R:21112186 (r6, Df).

Reference:

Parks et al., 2004, Nat. Genet. 36(3): 288--292

Associated Genes:

ca (allele - classic)

Associated Genes:

p (allele - classic)

Associated Genes:

st (allele - classic)